Cellular seeding and co-culture of a three dimensional fibroblast construct

ABSTRACT

The present invention provides methods for cellular seeding onto three-dimensional fibroblast constructs, three-dimensional fibroblast constructs seeded with muscle cells, and uses therefore.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. Ser. No. 15/943,322, filedApr. 2, 2018, allowed as U.S. Pat. No. 11,345,894, which is acontinuation of U.S. application Ser. No. 14/718,309, filed May 21,2015, issued as U.S. Pat. No. 9,976,123, which is a divisional of U.S.application Ser. No. 13/260,610, filed Feb. 7, 2012, issued as U.S. Pat.No. 9,051,550, which is a US national stage application of PCTApplication No. PCT/US10/30579 filed Apr. 9, 2012, which claims thebenefit of U.S. Provisional Patent Application Ser. No. 61/212,280 filedApr. 9, 2009, incorporated by reference herein in its entirety.

STATEMENT OF GOVERNMENT RIGHTS

This invention was made with government support under Merit Review Grant#0128, awarded by the U.S. Department of Veterans Affairs. Thegovernment has certain rights in the invention.

SEQUENCE LISTING STATEMENT

The sequence listing is filed in this application in electronic formatonly and is incorporated by reference herein. The sequence listing textfile “35642-US-5-CON_ST25.txt” was created on May 18, 2022, and is33,000 byte in size.

BACKGROUND

New treatments are needed for patients with chronic heart failure (CHF),the No. 1 hospital discharge diagnosis in patients over the age of 65years of age in this country, as well as related ischemic andnon-ischemic cardiac disorders. The prevalence of heart failure is over5 million; the incidence is 550,000 patients per year. Heart failureresults in more deaths than cancer, accidents, and strokes combined,costing more than $23 billion annually. Once a patient becomessymptomatic with NY Class III or IV heart failure, their mortalityapproaches 50% in two years without a heart transplant. The newestapproach to treat CHF is to inject stem cells and/or progenitor cellsdirectly into the heart using a number of different cell types. However,the results from recent clinical trials using such injection strategiesare generally disappointing.

SUMMARY OF THE INVENTION

In a first aspect, the present invention provides constructs comprisingmuscle cells adhered to a 3DFC, wherein the construct is capable ofspontaneous synchronized contractions across the 3DFC; and wherein themuscle cells are seeded on the construct at a density of between 0.5×10⁶cells/cm² and 5×10⁶ cells/cm² and/or the muscle cells are present in aratio of between about 1:10 and about 10:1 with fibroblasts on the 3DFC.In one embodiment, the muscle cells comprise cardiomyocytes or cardiacstem cells.

In a second aspect, the present invention provides methods for treatinga disorder characterized by a lack of functioning cardiomyocytes,comprising contacting the heart of a subject suffering from such adisorder with an amount effective to treat the disorder of a constructof any embodiment of the first aspect of the invention. In variousembodiments, the disorder is selected from the group consisting ofchronic heart failure (CHF), ischemia without heart failure,cardiomyopathy (such as dilated cardiomyopathy (DCM)), cardiac arrest,congestive heart failure, stable angina, unstable angina, myocardialinfarction, coronary artery disease, valvular heart disease, ischemicheart disease, reduced ejection fraction, reduced myocardial perfusion,maladaptive cardiac remodeling (such as left ventricle remodeling),reduced left ventricle function, left heart failure, right heartfailure, backward heart failure (increased venous back pressure),forward heart failure (failure to supply adequate arterial perfusion),systolic dysfunction, diastolic dysfunction, systemic vascularresistance, low-output heart failure, high-output heart failure, dyspneaon exertion, dyspnea at rest, orthopnea, tachypnea, paroxysmal nocturnaldyspnea, dizziness, confusion, cool extremities at rest, exerciseintolerance, easy fatigueability, peripheral edema, nocturia, ascites,hepatomegaly, pulmonary edema, cyanosis, laterally displaced apex beat,gallop rhythm, heart murmurs, parasternal heave, and pleural effusion.

In a third aspect, the present invention provides methods for seeding athree dimensional fibroblast construct (3DFC) with cells, comprising:

(a) contacting a cultured 3DFC with a suspension of cells to be seededonto the 3DFC;

(b) subjecting the cells within the suspension to a force that causessaid cells to contact the 3DFC; and

(c) culturing the cells under conditions suitable for the cells toadhere to the 3DFC.

In a fourth aspect, the present invention provides methods for seeding athree dimensional fibroblast construct (3DFC) with cells, comprising:

(a) contacting a cultured 3DFC with a cell sheet to be seeded onto the3DFC; and

(b) culturing the cell sheet under conditions suitable for the cellsheet to adhere to the 3DFC.

In a fifth aspect, the present invention provides constructs of anyembodiment of the first aspect of the invention made using the methodsof any embodiment of the third or fourth aspects of the invention.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1A-B: Endothelial progenitor cells tagged with CFDA-se co-culturedon 3DFC at A) 10 min and B) 24 hrs after seeding. Positively stainedCFDA-se tagged cells fluoresce green demonstrating additional cellsseeded on the 3DFC survive and proliferate. The biodegradable vicrylmesh can be seen in the background.

FIG. 2: Endothelial progenitor cells in a culture plate followingisolation of an intact cell sheet. Cells maintain all cell-to-celladhesion molecules and can be seeded and co-cultured onto the 3DFC.

FIG. 3A-C: Endothelial progenitor cell sheet after H&E stain. Darkpurple represents nuclei while the lighter pink indicates cytoplasm.Image shows (A) the full cell sheet (−8 mm diameter) and (B&C) highermagnification.

FIG. 4A-C: FIG. 4: 40× time elapsed images of control (A), NCM-3DFC (B),and NCM-3DFC+halothane (C) treated patches, cultured for 6 days andcontinuously injected with NBD. (A) Injection of a single fibroblast,note lack of dye transfer. (B) Injection of single neonatalcardiomyocyte on NCM-3DFC spreads to numerous neighboring cells. (C)Injection of a single neonatal cardiomyocyte on NCM-3DFC treated withhalothane. Note the disruption of dye transfer due to blockage ofconnexins by halothane. Cells regain ability to use gap junctions 15 to20 minutes after halothane treatment.

FIG. 5: Patches seeded with cardiomyocytes improved EF 25% in treatedvs. sham rats after 3 wks. Data are mean±SE/. NCM-3DFC=NeonatalCardiomyocyte 3DFC; SO=Sham Operated. SO, n=21; UN, n=12; 3DFC, n=9;NCM-3DFC, n=9. * P<0.05 vs SO; @ P<0.05 vs UN; #P<0.05 vs 3DFC.

FIG. 6: Patches seeded with cardiomyocytes improved cardiac index(ml/(min×grams)) 55% in treated vs. sham rats after 3 wks. Data aremean±SE. NCM-3DFC=Neonatal Cardiomyocyte 3DFC; SO=Sham Operated. SO,n=21; UN, n=12; 3DFC, n=9; NCM-3DFC, n=9. * P<0.05 vs SO; @ P<0.05 vsUN; #P<0.05 vs 3DFC.

FIG. 7: Patches seeded with cardiomyocytes improved end diastolicpressure (mmHg) in treated vs. sham rats after 3 wks. Data are mean±SE.NCM-3DFC=Neonatal Cardiomyocyte 3DFC; SO=Sham Operated. SO, n=19; UN(untreated), n=12; 3DFC, n=9; NCM-3DFC, n=9. * P<0.05 vs SO; @ P<0.05 vsUN; #P<0.05 vs 3DFC.

FIG. 8A-C: Hematoxylin and eosin stained 3DFC (A) and cardiomyocyteseeded 3DFC (B & C). 10× magnification of 3DFC (A) orientatedhorizontally. Vicryl bundles (in purple) and fibroblasts nucleiblue/purple dots. 5× magnification of cardiomyocyte seeded 3DFC (B)orientated horizontally. 10× magnification of cardiomyocyte seeded 3DFC(C) orientated horizontally. The large cellular bundles (B & C) consistof cardiomyocytes situated between vicryl fibers.

FIG. 9: 10× magnification H&E of 3DFC orientated horizontally. Vicrylbundles (in purple) and fibroblasts nuclei blue/purple dots.

FIG. 10: 5× magnification H&E of cardiomyocyte seeded 3DFC orientatedhorizontally. The large cellular bundles consist of cardiomyocytessituated between vicryl fibers.

FIG. 11: 10× magnification H&E of cardiomyocyte seeded 3DFC orientatedhorizontally. The large cellular bundles consist of cardiomyocytessituated between vicryl fibers.

DETAILED DESCRIPTION OF THE INVENTION

All references cited are herein incorporated by reference in theirentirety. Within this application, unless otherwise stated, thetechniques utilized may be found in any of several well-known referencessuch as: Molecular Cloning: A Laboratory Manual (Sambrook, et al., 1989,Cold Spring Harbor Laboratory Press), Gene Expression Technology(Methods in Enzymology, Vol. 185, edited by D. Goeddel, 1991. AcademicPress, San Diego, Calif.), “Guide to Protein Purification” in Methods inEnzymology (M. P. Deutshcer, ed., (1990) Academic Press, Inc.); PCRProtocols: A Guide to Methods and Applications (Innis, et al. 1990.Academic Press, San Diego, Calif.), Culture of Animal Cells: A Manual ofBasic Technique, 2nd Ed. (R. I. Freshney. 1987. Liss, Inc. New York,N.Y.), Gene Transfer and Expression Protocols, pp. 109-128, ed. E. J.Murray, The Humana Press Inc., Clifton, N.J.), and the Ambion 1998Catalog (Ambion, Austin, Tex.).

As used herein, the singular forms “a”, “an” and “the” include pluralreferents unless the context clearly dictates otherwise. “And” as usedherein is interchangeably used with “or” unless expressly statedotherwise.

All embodiments disclosed herein can be combined with other embodimentsunless the context clearly dictates otherwise.

In a first aspect, the present invention provides methods for seeding athree dimensional fibroblast construct (3DFC) with cells, comprising:

(a) contacting a cultured 3DFC with a suspension of cells to be seededonto the 3DFC;

(b) subjecting the cells within the suspension to a force that causesthe cells to contact the 3DFC; and

(c) culturing the cells under conditions suitable for the cells toadhere to the 3DFC.

The inventors have discovered that cells to be adhered to the 3DFC donot adequately settle out of solution onto the patch and adhere to the3DFC through cell-surface adhesion molecules. Early attempts at seedingthe 3DFC evaluated the placement of cells suspended in culture mediawith the notion that standard gravitational force would “settle” thedesired cells on the 3DFC below. Results found, poor retention of cellson the 3DFC with a majority of cells passing to the culture plate below.The inventors thus developed the methods of this first aspect of theinvention to force the cells to adhere to the surface of the 3DFC. Suchseeded 3DFC can be used, for example, in cell-based therapies, asdescribed in detail below.

As used herein, a “three dimensional fibroblast construct” is aconstruct comprising fibroblasts grown on a three-dimensional substratecomprising a biocompatible, non-living material formed into athree-dimensional structure having interstitial spaces bridged by thecells in the construct. It will be understood that the 3DFC may containcell types in addition to fibroblasts as appropriate for a givenpurpose. For example, the 3DFC may also comprise other stromal cells,including but not limited to endothelial cells. See, for example,published US patent application US2009/0269316 and U.S. Pat. No.4,963,489, both incorporated by reference herein in their entirety.

The fibroblasts and other cells may be fetal or adult in origin, and maybe derived from convenient sources such as skin, cardiac muscle, smoothmuscle, skeletal muscle, liver, pancreas, brain, adipose tissue (fat)etc. Such tissues and or organs can be obtained by appropriate biopsy orupon autopsy. In alternative embodiments for all aspects of theinvention, the fibroblasts and other cells are human cells. In analternative embodiment for all aspects of the invention, the 3DFC is amatrix-embedded human dermal construct of newborn dermal fibroblastscultured in vitro onto a bioabsorbable mesh to produce living,metabolically active tissue. The fibroblasts proliferate across the meshand secrete a large variety of growth factors and cytokines, includinghuman dermal collagen, fibronectin, and glycosaminoglycans (GAGs),embedding themselves in a self-produced dermal matrix. In culture thefibroblasts produce angiogenic growth factors: VEGF (vascularendothelial growth factor), HGF (hepatocyte growth factor), bFGF (basicfibroblast growth factor), and angiopoietin-1 (See, for example, J.Anat. (2006) 209, pp 527-532)

The cells to be seeded onto the 3DFC may be of any desired type,including but not limited to muscle cells (skeletal muscle cells, smoothmuscle cells, cardiac muscle cells such as cardiomyocyte) or progenitorsthereof, endothelial progenitor cells, bone marrow cells, bone marrowcells, mesenchymal stem cells, umbilical cord blood cells orcombinations thereof. Such cells can be isolated using standardtechniques in the art, or may be obtained from commercial sources.

In an alternative embodiment of all aspects of the invention, the seededcells comprise cardiomyocytes and/or progenitors thereof such as cardiacstem cells. There are a limited number of intrinsic cardiac stem cellsin the mature adult heart that are self-renewing, clonogenic, andmultipotent, such that they differentiate into cardiomyocytes and, to alesser extent, into smooth muscle and endothelial cells. Cardiac stemcells can be isolated and expanded in culture indefinitely. In oneembodiment, the cardiac stem cells are characterized by cell surfacemarkers: Lin−, c-Kit+, CD45−, CD34−.

The cells to be seeded may be recombinant cells capable of expressing agene product of interest for a given purpose. In one alternativeembodiment as described in more detail below, cardiomyocytes engineeredto express one or more of thymosin beta-4 (TB4), akt murine thyoma viraloncogene homolog (AKT1; SEQ ID NO:1, 3, or 5 for amino acid sequence),stroma cell-derived factor-1 alpha (SDF-1; SEQ ID NO:7 for amino acidsequence), and hepatocyte growth factor (HGF; SEQ ID NO:9 for amino acidsequence) are seeded onto the 3DFC. Techniques for engineering cells toexpress a heterologus gene product are well known in the art, andutilize cell transfection by recombinant expression vector thatoperatively link a nucleic acid coding region or gene to any promotercapable of effecting expression of the gene product. Thus, in variousembodiments, the cells comprise a recombinant expression vector encodinga nucleic acid sequence that encodes the polypeptide sequence one ormore of SEQ ID NO:1, 3, 5, 7, 9, and 11, In various further embodiments,the nucleic acid sequence is selected from the group consisting of SEQID NOS: 2, 4, 6, 8, and 10. The promoter sequence used to driveexpression of the disclosed nucleic acid sequences in a mammalian systemmay be constitutive (driven by any of a variety of promoters, includingbut not limited to, CMV, SV40, RSV, actin, EF, etc.) or inducible(driven by any of a number of inducible promoters including, but notlimited to, tetracycline, ecdysone, steroid-responsive). See, forexample, Sambrook, Fritsch, and Maniatis, in: Molecular Cloning, ALaboratory Manual, Cold Spring Harbor Laboratory Press, 1989; GeneTransfer and Expression Protocols, pp. 109-128, ed. E. J. Murray, TheHumana Press Inc., Clifton, N.J.), and the Ambion 1998 Catalog (Ambion,Austin, Tex.).

Contacting a cultured 3DFC with a suspension of cells to be seeded ontothe 3DFC can be done under any suitable conditions to facilitateapplication of the force that causes the cells to contact the 3DFC,including but not limited to the conditions described below. In onealternative embodiment, the 3DFC is placed in 0.1 to 5 ml of media(preferably 0.25 ml-2 ml, and more preferable 0.5 ml-1.0 ml of media),and cells are introduced in suspension, such that the volume of cellsuspension is approximately double the volume of media in which the 3DFCis placed. In one alternative embodiment that can be combined with anyother embodiments herein, the contacting occurs at approximately 37° C.In a further alternative embodiment that can be combined with any otherembodiments herein, the cell suspension has a concentration of at least3×10 ⁶ cells/ml where the cells to be seeded are contractile cells (suchas cardiomyocytes or progrenitors thereof). In further alternativeembodiments that can be combined with any other embodiments herein, thecell suspension has a concentration of at least 4×10 ⁶ cells/ml and 5×10⁶ cells/ml.

In one embodiment, each 3DFC to be seeded is placed in a well so as tocover the base of the well and lay flat. The inventors have discoveredthat if the 3DFC does not cover the base of the well (when seeding 3DFCsplaced in wells), a decreased retention of cells occurs, and results inan unequal distribution of cells across the patch due to cell bunchingand clumping.

Subjecting the cells within the suspension to a force that causes saidcells to contact the 3DFC may comprise the use of any suitable force,including but not limited to a centrifugal force and an electrical forcegenerated by an electric field, or combinations of such forces. In analternative embodiment, a centrifugal force is used. The centrifugalforce to be applied depends on a variety of factors, such as the celltype to be seeded onto the 3DFC. In one alternative embodiment that canbe combined with any other embodiments herein, the construct iscentrifuged at between 1200 rpms and 1600 rpms for between 2 and 10minutes. In an alternative embodiment, all 3DFC constructs to be seededare placed in a horizontal arrangement in wells (as opposed tovertical), so that each well is spun at the same radius.

In one alternative embodiment, the force may be applied within 0-300seconds after contacting of the cell suspension with the 3DFC inappropriate culture medium.

It will be understood by those of skill in the art that it is not arequirement that all cells in the suspension contact the 3DFC as aresult of the force application, as the cells can preferably be presentin the suspension in an amount that saturates all available locationsfor seeding onto the 3DFC. In one alternative embodiment, the seededcells contact each other, such that multiple cell layers are provided ontop of the 3DFC. In embodiments where cardiomyocytes or precursorsthereof are used, it is preferred that the seeded cells reside in the“valleys” between fibers on the 3DFC (see below for description of 3DFCstructure). Exemplary images of such cardiomyocyte-seeded 3DFCs areshown in FIGS. 8-11.

Culturing the cells under conditions suitable for the cells to adhere tothe 3DFC may comprise the use of any culture media and conditionssuitable for a given purpose, such as those in the examples that follow.Any useful media may be used, including but not limited to DMEM-LGsupplemented with fetal bovine serum (5-15%; preferably 10%) and otherappropriate factors (including but not limited to sodium bicarbonate andantibiotics. It will be understood by those of skill in the art that itis not a requirement that all cells in the suspension adhere to the 3DFCas a result of the force application, as the cells can preferably bepresent in the suspension in an amount that saturates all availablelocations for adherence onto the 3DFC. In an alternative embodiment thatcan be combined with any other embodiment disclosed herein, the cellsare adhered to the 3DFC at a cell density ranging between 0.5×10 ⁶cells/cm² and 5×10 ⁶ cells/cm²; more preferably between 1×10 ⁶ cells/cm²and 4×10 ⁶ cells/cm²; and most preferably between 1.5×10 ⁶ cells/cm² and3×10 ⁶ cells/cm².

In a further alternative embodiment that can be combined with any of theother embodiments disclosed herein, the culturing further comprisesgrowth of cells adhered to the 3DFC. In this embodiment, such growth canoccur under the same or different culture conditions than those used topromote adherence of the suspended cells to the 3DFC. Suitable cultureconditions to promote proliferation and/or differentiation of cellsadhered to the 3DFC can be determined by those of skill in the art,based on the disclosure herein.

In another alternative embodiment that can be combined with any otherembodiment herein, the seeded 3DFCs are incubated within 5 minutes ofapplication of force and not disturbed (i.e. the 3DFCs are not removedfrom culture plate, media changed, etc.). Seeded 3DFCs for in vivoimplant are preferably harvested from culture plates ˜18-20 hrs afterseeding/incubation.

Exemplary methods for seeding are provided in the examples that follow.The 3DFC may be purchased from commercial sources (ANGINERA™ (Theregen,Inc., California); Advanced BioHealing, Inc (DERMAGRAFT®)), or may beprepared as described, for example, in US2009/0269316 and U.S. Pat. No.4,963,489. Briefly, fibroblasts and, optionally, other stromal cells asdeemed appropriate for a given purpose, are inoculated upon athree-dimensional framework, and grown to develop the 3DFC. Thefibroblasts and other stromal cells may be engineered to express geneproducts of interest, such as thymosin beta 4. See, for example, U.S.Pat. Nos. 5,785,964 and 5,957,972, incorporated by reference herein intheir entirety.

The three-dimensional support framework may be of any material and/orshape that: (a) allows cells to attach to it (or can be modified toallow cells to attach to it); and (b) allows cells to grow in more thanone layer. A number of different materials may be used to form theframework, including but not limited to: nylon (polyamides), dacron(polyesters), polystyrene, polypropylene, polyacrylates, polyvinylcompounds (e.g., polyvinylchloride; PVC), polycarbonate,polytetrafluorethylene (PTFE; TEFLON), thermanox (TPX), nitrocellulose,cotton, polyglycolic acid (PGA), cat gut sutures, cellulose, gelatin,dextran, etc. Any of these materials may be woven into a mesh to formthe three-dimensional framework. Certain materials, such as nylon,polystyrene, etc., are poor substrates for cellular attachment. Whenthese materials are used as the three-dimensional support framework, itis advisable to pre-treat the framework prior to inoculation offibroblasts and other stromal cells in order to enhance their attachmentto the framework. For example, prior to inoculation with fibroblasts andother stromal cells, nylon screens could be treated with 0.1 M aceticacid, and incubated in polylysine, fetal bovine serum, and/or collagento coat the nylon. Polystyrene could be similarly treated using sulfuricacid.

When the 3DFC is to be implanted directly in vivo, it may be preferableto use biodegradable materials such as PGA, catgut suture material,collagen, polylactic acid, or hyaluronic acid. For example, thesematerials may be woven into a three-dimensional framework such as acollagen sponge or collagen gel. Where the cultures are to be maintainedfor long periods of time or cryopreserved, non-degradable materials suchas nylon, dacron, polystyrene, polyacrylates, polyvinyls, teflons,cotton, etc. may be preferred. A convenient nylon mesh which could beused in accordance with the invention is a nylon filtration mesh havingan average pore size of 140 μm and an average nylon fiber diameter of 90μm (#3-210/36, Tetko, Inc., N.Y.).

Stromal cells comprising fibroblasts, with or without other cells andelements described below, are inoculated onto the framework. Thesestromal cells may be derived from tissues or organs, such as skin,heart, blood vessels, skeletal muscle, liver, pancreas, brain etc.,which can be obtained by biopsy (where appropriate), from surgicallyobtained specimens, or upon autopsy. Fetal fibroblasts can be used toform a “generic” three-dimensional stromal tissue that will support thegrowth of a variety of different cells and/or tissues that come incontact with it. However, a “specific” stromal tissue may be prepared byinoculating the three-dimensional framework with stromal cells derivedfrom the heart and/or from a particular individual who is later toreceive the cells and/or tissues grown in culture in accordance with thepresent invention. Such samples can be obtained, for example, throughstandard biopsy procedures (such as a myocardial biopsy when stromalcells from the heart are to be obtained) or other surgical procedure.

Stromal cells may be readily isolated by disaggregating an appropriateorgan or tissue. This may be readily accomplished using techniques knownto those skilled in the art. For example, the tissue or organ can bedisaggregated mechanically and/or treated with digestive enzymes and/orchelating agents that weaken the connections between neighboring cellsmaking it possible to disperse the tissue into a suspension ofindividual cells without appreciable cell breakage. Enzymaticdissociation can be accomplished by mincing the tissue and treating theminced tissue with any of a number of digestive enzymes either alone orin combination. These include, but are not limited to, trypsin,chymotrypsin, collagenase, elastase, and/or hyaluronidase, DNase,pronase, and dispase. Mechanical disruption can also be accomplished bya number of methods including, but not limited to, the use of grinders,blenders, sieves, homogenizers, pressure cells, or insonators to namebut a few. For a review of tissue disaggregation techniques, seeFreshney, Culture of Animal Cells. A Manual of Basic Technique, 2d Ed.,A. R. Liss, Inc., New York, 1987, Ch. 9, pp. 107-126.

Once the tissue has been reduced to a suspension of individual cells,the suspension can be fractionated into subpopulations from which thefibroblasts and/or other stromal cells and/or elements can be obtained.This also may be accomplished using standard techniques for cellseparation including, but not limited to, cloning and selection ofspecific cell types, selective destruction of unwanted cells (negativeselection), separation based upon differential cell agglutinability inthe mixed population, freeze-thaw procedures, differential adherenceproperties of the cells in the mixed population, filtration,conventional and zonal centrifugation, centrifugal elutriation(counter-streaming centrifugation), unit gravity separation,countercurrent distribution, electrophoresis and fluorescence-activatedcell sorting. For a review of clonal selection and cell separationtechniques, see Freshney, Culture of Animal Cells. A Manual of BasicTechniques, 2d Ed., A. R. Liss, Inc., New York, 1987, Ch. 11 and 12, pp.137-168.

Where the cultured cells are to be used for transplantation orimplantation in vivo, it is preferable to obtain the stromal cells fromthe patient's own tissues.

After inoculation of the stromal cells, the 3DFC should be incubated inan appropriate nutrient medium. Many commercially available media suchas RPMI 1640, Fisher's, Iscove's, McCoy's, and the like may be suitablefor use. In an alternative embodiment, the 3DFC may be suspended in themedium during the incubation period in order to maximize proliferativeactivity of the fibroblasts and other stromal cells. In addition, theculture should be “fed” periodically to remove the spent media,depopulate released cells, and add fresh media. During the incubationperiod, the fibroblasts and other stromal cells will grow linearly alongand envelop the filaments of the three-dimensional framework beforebeginning to grow into the openings of the framework.

The openings of the framework should be of an appropriate size to allowthe fibroblasts and other stromal cells to stretch across the openings.Maintaining actively growing stromal cells that stretch across theframework enhances the production of growth factors that are elaboratedby the stromal cells, and hence will support long term cultures. Forexample, if the openings are too small, the stromal cells may rapidlyachieve confluence but be unable to easily exit from the mesh; trappedcells may exhibit contact inhibition and cease production of theappropriate factors necessary to support proliferation and maintain longterm cultures. If the openings are too large, the stromal cells may beunable to stretch across the opening; this will also decrease stromalcell production of the appropriate factors necessary to supportproliferation and maintain long term cultures. When using a mesh type offramework, as exemplified herein, it has been found that openingsranging from about 140 μm to about 220 μm will work satisfactorily.However, depending upon the three-dimensional structure and intricacy ofthe framework, other sizes may work equally well. In fact, any shape orstructure that allows the stromal cells to stretch and continue toreplicate and grow for lengthy time periods will work in accordance withthe invention.

Different proportions of the various types of collagen deposited on theframework can affect the growth of the cells that come in contact withthe 3DFC. The proportions of extracellular matrix (ECM) proteinsdeposited can be manipulated or enhanced by selecting fibroblasts thatelaborate the appropriate collagen type. This can be accomplished usingmonoclonal antibodies of an appropriate isotype or subclass that arecapable of activating complement, and which define particular collagentypes. These antibodies and complement can be used to negatively selectthe fibroblasts which express the desired collagen type. Alternatively,the stroma used to inoculate the framework can be a mixture of cellswhich synthesize the appropriate collagen types desired. Thus, since the3DFC described herein is suitable for the growth of diverse cell typesand tissues, and depending upon the tissue to be cultured and thecollagen types desired, the appropriate stromal cell(s) may be selectedto inoculate the three-dimensional framework.

During incubation of the 3DFC, proliferating cells may be released fromthe framework. These released cells may stick to the walls of theculture vessel where they may continue to proliferate and form aconfluent monolayer. This should be prevented or minimized, for example,by removal of the released cells during feeding, or by transferring the3DFC to a new culture vessel. The presence of a confluent monolayer inthe vessel may “shut down” the growth of cells in the 3DFC. Removal ofthe confluent monolayer or transfer of the stromal tissue to fresh mediain a new vessel will restore proliferative activity of the 3DFC. Suchremoval or transfers should be done in any culture vessel which has astromal monolayer exceeding 25% confluency. Alternatively, the 3DFCcould be agitated to prevent the released cells from sticking, orinstead of periodically feeding the cultures, the culture system couldbe set up so that fresh media continuously flows through the 3DFC. Theflow rate could be adjusted to both maximize proliferation within the3DFC, and to wash out and remove cells released from the culture, sothat they will not stick to the walls of the vessel and grow toconfluence.

In a second aspect, the present invention provides methods for seeding athree dimensional fibroblast construct (3DFC) with cells, comprising:

(a) contacting a cultured 3DFC with a cell sheet to be seeded onto the3DFC; and

(b) culturing the cell sheet under conditions suitable for the cellsheet to adhere to the 3DFC.

The inventors have unexpectedly discovered that the methods of thisaspect of the invention permit the harvest of cells sheets for seedingonto a 3DFC, and thus permit their use as a delivery method, such as themethods disclosed below for treating chronic heart failure.

In one alternative embodiment, cell sheets with cardiac stem cells areadhered to the 3DFC, allowing cardiac stem cells to establish andmaintain cellular/electrical communications such as gap junctions priorto placement onto the myocardium in the methods of the invention fortreating CHF, discussed in more detail below.

All terms in this second aspect are as defined for the first aspect ofthe invention, and all embodiments of the first aspect of the inventionare equally applicable to this second aspect of the invention. In thissecond aspect, the 3DFC is contacted with a cell sheet under conditionssuitable for adherence to the 3DFC. As used herein, a “cell sheet”comprises confluent cells dissociated from culture as an intact “sheet”for contacting with the 3DFC. In an alternative embodiment, thedisassociating is effected by chilling the culture substrate to atemperature effective to release said cells as an intact cell sheet; anysuitable temperature may be used, preferably between 10-20° C.

Contacting a cultured 3DFC with a cell sheet to be seeded onto the 3DFCand subsequent culturing to promote cell sheet adherence to the 3DFC canbe done under any suitable conditions, such as those described in theexamples that follow, and those discussed with respect to the firstaspect of the invention. Based on the teachings herein, those of skillin the art can determine appropriate conditions for contacting thecultured 3DFC with the cell sheet to be seeded onto the 3DFC; andculturing the cell sheet under conditions suitable for the cell sheet toadhere to the 3DFC. In one exemplary alternative embodiment, the cellsof interest are grown in culture until confluency, followed by chillingof the culture substrate to approximately 10° C.-20° C.), which allowsdissociation of the cell sheet from the culture substrate. Dissociationis generally complete within (30-60 minutes, and the dissociated cellsheet is taken up by any suitable means, such as by appropriately sizedpipette and transferred onto the 3DFC. In one alternative embodiment, asuitable amount of culture media (1-5 μl; preferably 2-3 ul) is placedonto the cell sheet so that it unfolds to lay flat against the 3DFC. Anysuitable cell media may be used, including but not limited to DMEMsupplemented with 5-15% fetal bovine serum (preferably approximately10%). After the cell sheet is relatively flattened and is flush againstthe 3DFC excess media is removed using a pipette. The 3DFC cell sheetcomplex is placed in the incubator for 5 min at 5.0% CO₂ and 37 degreesC. After which, the 3DFC cell sheet complex is re-suspended in 37 degreeC. 10% FBS in DMEM and cultured overnight. The cell sheet is preferablycentrally placed on the 3DFC, and is placed so as to minimize folds orbunching in the cell sheet, The construct is then incubated underappropriate conditions to promote adhesion of the cells in the cellsheet to the 3DFC. Any suitable conditions can be used. In onealternative embodiment that can be combined with any other embodimentsherein, the incubation occurs at 37° C. and 5% CO₂ for between 5 and 15minutes; more preferably between 7.5 and 12.5 minutes; most preferablyapproximately 10 minutes.

In a further alternative embodiment, the desired cells are grown andcultured in temperature sensitive plates under standard cultureconditions. Once confluent, cell media volume is reduced by 50% and theplates are chilled at 20 degrees C. for 30-60 min or until cell sheetsdissociate from the culture plate. Using a pipette, cell sheets areharvested, placed on thawed 3DFC and flattened using droplets ofstandard culture media. Once flattened, excess media is removed using apipette. The 3DFC cell sheet complex is placed in the incubator (5.0%CO₂ at 37° C. for 5 min. 3DFC cell sheet complex is re-suspended in 37°C. standard culture medium, placed back in the incubator and culturedover night. Culture media is changed every 48 hrs.

Any suitable initial seeding densities in the temperature sensitiveculture plates can be used, and may vary on cell type. In onealternative embodiment, cardiomyocytes or precursors thereof are seededat approximately 1-2×10⁴ cells/mm²; preferably approximately 1.4×10⁴cells/mm².

The cells in the cell sheet may be of any desired type, including butnot limited to muscle cells (skeletal muscle cells, smooth muscle cells,cardiac muscle cells such as cardiomyocyte) and progenitors thereof,endothelial progenitor cells, bone marrow cells, umbilical cord bloodcells, and combinations thereof. In an alternative embodiment cell typeswith strong cell-cell interactions, such as endothelial cells andcardiomyocytes or progenitors thereof, are used.

In an alternative embodiment of all aspects of the invention, the seededcells comprise cardiomyocytes and/or progenitors thereof such as cardiacstem cells. There are a limited number of intrinsic cardiac stem cellsin the mature adult heart that are self-renewing, clonogenic, andmultipotent, such that they differentiate into cardiomyocytes and, to alesser extent, into smooth muscle and endothelial cells. Cardiac stemcells can be isolated and expanded in culture indefinitely and arecharacterized by cell surface markers: Lin−, c-Kit+, CD45-, CD34-. See,for example, Messina et al., Circulation Research, 2004, 95:911; Barileet al., Nat. Clin. Prac. Cardiovasc. Med. 2007, Feb. 4, Suppl 1: S9-S14;Noort et al., Pediatric Cardiology, 30(5):699 (2009); Cardiac stem cellisolation kit available from Millipore (Cat. #SCR061)

The cells to be seeded may be recombinant cells capable of expressing agene product of interest for a given purpose. In one alternativeembodiment as described in more detail below, cardiomyocytes engineeredto express thymosin beta-4 are seeded onto the 3DFC.

It will be understood by those of skill in the art that it is not arequirement that all cells in the cell sheet contact the 3DFC. In onealternative embodiment, the seeded cell sheets may contact each other,to yield two or more cell layers atop the 3DFC. It will be understood bythose of skill in the art that it is not a requirement that all cells inthe cell sheet adhere to the 3DFC as a result of the force application,as the cells are preferably present in the suspension in an amount thatsaturates all available locations for adherence onto the 3DFC. In analternative embodiment that can be combined with any other embodimentdisclosed herein, the cells are adhered to the 3DFC at a cell densityranging between 0.5×10⁶ cells/cm² and 5×10⁶ cells/cm²; more preferablybetween 1×10⁶ cells/cm² and 4×10⁶ cells/cm²; and most preferably between1.5×10⁶ cells/cm² and 3×10⁶ cells/cm².

In a further alternative embodiment that can be combined with any of theother embodiments disclosed herein, the culturing further comprisesgrowth of cells adhered to the 3DFC. In this embodiment, such growth canoccur under the same or different culture conditions than those used topromote adherence of the cell sheet to the 3DFC. Suitable cultureconditions to promote proliferation and/or differentiation of cellsadhered to the 3DFC can be determined by those of skill in the art,based on the disclosure herein. Once adhesion of the sheet occurs, the3DFC cell sheet complex can be cultured under standard culture methods.

In a third aspect, the present invention provides constructs comprisingmuscle cells adhered to a 3DFC, wherein the cells are capable ofspontaneous synchronized contractions across the 3DFC; and wherein themuscle cells are seeded on the construct at a density of between 0.5×10⁶cells/cm² and 5×10⁶ cells/cm² and/or the muscle cells are present in aratio of between about 1:10 and about 10:1 with fibroblasts on theconstruct. Terms in this third aspect of the invention retain themeaning disclosed in the first and second aspects of the invention. Allembodiments of the first and second aspects of the invention are equallyapplicable to this third aspect of the invention, unless the contextclearly indicates otherwise. In another embodiment, fibroblasts arepresent on the construct at a density of between about 5.0×10⁵ cells/cm²and about 5.0×10⁶ cells/cm²; in another embodiment between about 8.0×10⁵cells/cm² and about 2.0×10⁶ cells/cm².

As discussed in more detailed below, the inventors have discovered thatthe constructs of this aspect of the invention can be used, for example,in cell therapy for treating various disorders such as chronic heartfailure. The inventors have further discovered that the resultingconstruct provides for cell-cell communication across the construct,which can beat synchronously.

In one alternative embodiment, the 3DFC comprises a patch, with thecells seeded onto a top portion of the patch. In this embodiment, thebottom portion of the patch can be attached to a surface of interest,such as the heart.

The constructs of the invention comprise muscle cells are seeded on theconstruct at a density of between 0.5×10⁶ cells/cm² and 5×10⁶ cells/cm²and/or muscle cells are present in a ratio about of between 1:10 andabout 10:1 with fibroblasts on the construct. In one embodiment, musclecells are seeded on the construct at a density of between 1.5×10⁶cells/cm² 3.0×10⁶ cells/cm². In another embodiment, the muscle cells arepresent in a ratio of between about 1:10 and about 10:1 with fibroblastson the construct. In another embodiment, the muscle cells are seeded onthe construct at a density of between 0.5×10⁶ cells/cm² and 5×10⁶ andthe muscle cells are present in a ratio of between 1:10 and 10:1 withfibroblasts on the construct. In a preferred embodiment of all theseembodiments, the muscle cells are cardiomyocytes or precursors thereof.

In various embodiments, the muscle cells (such as cardiomyocytes orprecursors thereof) are present in a ratio with fibroblasts on theconstruct of between about 1:10 and about 10:1; about 1:9 to about 9:1;about 1:8 to about 8:1; about 1:7 to about 7:1; about 1:6 to about 6:1;about 1:5 to about 5:1; about 1:4 to about 4:1; about 1:3 to about 3:1;about 1:2 to about 2:1; or about 1:1. Other ratios of cells are alsopossible. In a preferred embodiment of all these embodiments, the musclecells are cardiomyocytes or precursors thereof.

In various embodiments, the muscle cells (such as cardiomyocytes orprecursors thereof) are seeded on the construct at a density between1.3×10⁶ cells/cm² and 5×10⁶ cells/cm²; more preferably between 1.4×10⁶cells/cm² and 4×10⁶ cells/cm²; and most preferably between 1.5×10⁶cells/cm² and 3×10⁶ cells/cm². In a preferred embodiment of all theseembodiments, the muscle cells are cardiomyocytes or precursors thereof.

In another embodiment, the cardiomyocytes or precursors thereof areseeded on the construct at a density between 1.5×10⁶ cells/cm² and 3×10⁶cells/cm², and the fibroblasts are present on the construct at a densityof between about 8.0×10⁵ cells/cm² and about 2.0×10⁶ cells/cm².

As used herein, “muscle cells” can be skeletal muscle cells, smoothmuscle cells, cardiac muscle cells, or precursors thereof. In analternative embodiment that can be combined with any other embodimentherein, the muscle cells comprise cardiomyocytes or precursors thereof;most preferably of human origin. In a further alternative embodimentthat can be combined with any other embodiment, the construct is aseeded, non-contracting patch, which can be ready for implantation by 24hours after seeding and used, for example, to provide cardiomyocytes tothe host heart. In another alternative embodiment that can be combinedwith any other embodiment, the construct is a contractile construct, iscapable of spontaneous synchronized contractions, and may be used, forexample, for contractile assistance. As used herein, the phrase“spontaneous synchronized contractions” means that the cells are capableof producing coordinated force generation across the 3DFC. As usedherein, “across the 3DFC” means that the cells are capable ofspontaneous synchronized contractions over the full 3DFC where the cellsare adhered.

In a further alternative embodiment that can be combined with any otherembodiment herein, the muscle cells, or precursors thereof, are obtainedfrom a subject (such as by standard biopsy procedures or other surgicalprocedures) to be treated with the construct in the methods of theinvention described below. In a further alternative embodiment that canbe combined with any other embodiment herein, the cells can beengineered to express a protein of interest, such as cardiomyocytes orprecursors thereof engineered to express one or more of thymosin beta-4(TB4), akt murine thyoma viral oncogene homolog (AKT1; SEQ ID NO:1, 3,or 5 for amino acid sequence), stroma cell-derived factor-1 alpha(SDF-1; SEQ ID NO:7 for amino acid sequence), and hepatocyte growthfactor (HGF; SEQ ID NO:9 for amino acid sequence), as disclosed above.

The constructs can be made shortly prior (ie, 0-10 days prior) to adesired implantation according to the methods of the invention describedbelow, or may be stored frozen and rethawed prior to implantation.

The muscle cells can be adhered to the 3DFC at any density suitable fora given application. In an alternative embodiment that can be combinedwith any other embodiment disclosed herein, the muscle cells (such ascardiomyocytes or precursors thereof) are adhered to the 3DFC at a celldensity ranging between 1.3×10⁶ cells/cm² and 5×10⁶ cells/cm²; morepreferably between 1.4×10⁶ cells/cm² and 4×10⁶ cells/cm²; and mostpreferably between 1.5×10⁶ cells/cm² and 3×10⁶ cells/cm². Lower densitycardiomyocyte seedings (0.6-1.2×10⁶ cells/cm²) displayednon-synchronized yet spontaneous contractions, while higher densityconstructs disclosed were capable of consistent rhythmic and directionalcontractions

Specific methods for producing constructs according to this aspect ofthe invention are provided in the examples that follow. In oneembodiment, the methods of any embodiment or combination of embodimentsof the first or second aspect of the invention can be used to make theconstructs of this third aspect. In one alternative embodiment, cellsheets with cardiac stem cells or cardiomyocytes are adhered to the3DFC, allowing cardiac stem cells or cardiomyocytes to which they giverise to establish and maintain cellular/electrical communications suchas gap junctions prior to placement onto the myocardium in the methodsof the invention for treating CHF, discussed in more detail below.

In a fourth aspect, the present invention provides methods for treatinga disorder characterized by a lack of functioning cardiomyocytes,comprising contacting the heart of a subject suffering from such adisorder with an amount effective to treat the disorder of a constructaccording to the third aspect of the invention that comprisecardiomyocytes or precursors thereof adhered to a 3DFC.

The inventors have unexpectedly discovered that the constructs of thisaspect of the invention can be used, for example, in cell therapy fortreating disorders characterized by a lack of functioningcardiomyocytes. Such disorders include, but are not limited to, chronicheart failure (CHF), ischemia without heart failure, cardiomyopathy(such as dilated cardiomyopathy (DCM)), cardiac arrest, congestive heartfailure, stable angina, unstable angina, myocardial infarction, coronaryartery disease, valvular heart disease, ischemic heart disease, reducedejection fraction, reduced myocardial perfusion, maladaptive cardiacremodeling (such as left ventricle remodeling), reduced left ventriclefunction, left heart failure, right heart failure, backward heartfailure (increased venous back pressure), forward heart failure (failureto supply adequate arterial perfusion), systolic dysfunction, diastolicdysfunction, systemic vascular resistance, low-output heart failure,high-output heart failure, dyspnea on exertion, dyspnea at rest,orthopnea, tachypnea, paroxysmal nocturnal dyspnea, dizziness,confusion, cool extremities at rest, exercise intolerance, easyfatigueability, peripheral edema, nocturia, ascites, hepatomegaly,pulmonary edema, cyanosis, laterally displaced apex beat, gallop rhythm,heart murmurs, parasternal heave, and pleural effusion. In oneembodiment the disorder is CHF; in another embodiment the disorder isDCM. In another embodiment, the disorder is ischemia without heartfailure. While not being bound by any mechanism of action, the inventorsbelieve that current failure of cell therapy efforts to treat disorderssuch as CHF (based at least in part on the lack of survival of implantedstem cells) is related to trying to grow cells in a hostile environmentwithout adequate blood supply/matrix support. Without adequateextracellular matrix, injected cells clump due to lack of physicalsupport for the cells to attach. In contrast, co-populating the 3DFCwith cardiomyocytes and/or cardiac stem cells as per the methods of thepresent invention will enable these cells to grow and engraft onto theheart. This coupled with improved blood flow will result in more viablemyocardium to treat the disorders disclosed above, for example, throughimproved left ventricular (LV) function and reduced maladaptive LVremodeling. The 3DFC provides growth factor stimulation to enhancematrix support/new blood vessel formation allowing cardiomyocytes and/orcardiac stem cells to engraft and grow. Fibroblasts in the 3DFC produceangiogenic growth factors: VEGF (vascular endothelial growth factor),HGF (hepatocyte growth factor), bFGF (basic fibroblast growth factor),and angiopoietin-1 (See, for example, J. Anat. (2006) 209, pp 527-532),which also help to provide vasculature for survival of the seededcardiomyocytes. Thus, a significant advantage of the co-culture on 3DFCis that the 3DFC is pro-angiogenic or pro-arteriogenic, and thusaddresses ischemia at the same time the co-cultured patch is deliveringcells or beating function to the heart. Thus, the underlying 3DFC makesthe ischemic myocardium more friendly to the seeded cells and thus morelikely to survive and become functional, which can include migrating offthe construct to functionally integrate into the myocardium, orremaining on the construct. As will be clear to those of skill in theart, the construct also can be used as an adjunct therapy, to provide apumping assist without integration of the cardiomyocytes into the heartmyocardium.

Thus, in a further alternative embodiment that can be combined with anyother embodiment herein, the construct is a seeded, non-contracting 3DFCpatch to provide cardiomyocytes to the host heart and to becomefunctional or to functionally integrate into the myocardium. In anotheralternative embodiment that can be combined with any other embodimentherein, the construct is a contractile construct and may be used, forexample, as an adjunct therapy, to provide a pumping assist withoutintegration of the cardiomyocytes into the heart myocardium.

In the methods of the invention, attaching the matrix scaffold to theheart subjects it to mechanical stress that stimulates cell migration,growth, and secretion of extracellular matrix protein. The rhythmicstretching of the scaffold facilitates nutrient and waste exchangewithin the scaffold by opening and compressing the scaffold pores.

Thus, the present methods utilize the 3DFC as a delivery system forcell-based therapy using the heart as its own bioreactor to support theengraftment/growth of cells seeded on the 3DFC. The methods of theinvention permit covering a larger amount of myocardium as opposed toisolated cell injections, thus addressing one criticism as to why cellinjections appear to work better in rodents than humans, ie., the amountof damaged myocardium needed to treat. Also cells seeded on the 3DFCwill not wash out in the circulation as seen with insolated cellinjections.

In an alternative embodiment that can be combined with any otherembodiments herein, the subject is a mammal, most preferably a human. Ina further alternative embodiment that can be combined with any otherembodiments herein, the subject is human. In another alternativeembodiment, the cardiomyocytes or cardiac stem cells are obtained fromthe subject.

As used herein, “CHF” is a chronic (as opposed to rapid onset)impairment of the heart's ability to supply adequate blood to meet thebody's needs. CHF may be caused by, but is distinct from, cardiacarrest, myocardial infarction, and cardiomyopathy. In one alternativeembodiment, the subject suffers from congestive heart failure. Invarious further alternative embodiments that can be combined with anyother embodiments herein, the subject's heart failure comprises leftheart failure, right heart failure, backward heart failure (increasedvenous back pressure), forward heart failure (failure to supply adequatearterial perfusion), systolic dysfunction, diastolic dysfunction,systemic vascular resistance, low-output heart failure, high-outputheart failure. In various further alternative embodiments that can becombined with any other embodiments herein, the subject's CHF may be anyof Classes I-IV as per the New York Heart Association FunctionalClassification; more preferably Class III or IV.

-   -   Class I: no limitation is experienced in any activities; there        are no symptoms from ordinary activities.    -   Class II: slight, mild limitation of activity; the patient is        comfortable at rest or with mild exertion.    -   Class III: marked limitation of any activity; the patient is        comfortable only at rest.    -   Class IV: any physical activity brings on discomfort and        symptoms occur at rest.

In a further alternative embodiment that can be combined with any otherembodiments herein, the subject has been diagnosed with CHF according tothe New York Heart Association Functional Classification. In a furtheralternative embodiment that can be combined with any other embodimentsherein, the subject is further characterized by one or more of thefollowing: hypertension, obesity, cigarette smoking, diabetes, valvularheart disease, and ischemic heart disease.

As used herein, “treat” or “treating” means accomplishing one or more ofthe following: (a) reducing the severity of the disorder (ex: treatmentof Class IV subject to improve status to Class III for CHF subjects);(b) limiting or preventing development of symptoms characteristic of thedisorder; (c) inhibiting worsening of symptoms characteristic of thedisorder; (d) limiting or preventing recurrence of symptoms in patientsthat were previously symptomatic for the disorder. Signs characteristicof CHF include, but are not limited to reduced ejection fraction,reduced myocardial perfusion, maladaptive cardiac remodeling (such asleft ventricle remodeling), reduced left ventricle function, dyspnea onexertion, dyspnea at rest, orthopnea, tachypnea, paroxysmal nocturnaldyspnea, dizziness, confusion, cool extremities at rest, exerciseintolerance, easy fatigueability, peripheral edema, nocturia, ascites,hepatomegaly, pulmonary edema, cyanosis, laterally displaced apex beat,gallop rhythm, heart murmurs, parasternal heave, and pleural effusion.

In one embodiment, the constructs described herein find use in promotingthe healing of ischemic heart tissue. The ability of the constructs topromote the healing of an ischemic tissue depends in part, on theseverity of the ischemia. As will be appreciated by the skilled artisan,the severity of the ischemia depends, in part, on the length of time thetissue has been deprived of oxygen. Among such activities is thereduction or prevention of the remodeling of ischemic tissue. By“remodeling” herein is meant, the presence of one or more of thefollowing: (1) a progressive thinning of the ischemic tissue, (2) adecrease in the number or blood vessels supplying the ischemic tissue,and/or (3) a blockage in one or more of the blood vessels supplying theischemic tissue, and if the ischemic tissue comprises muscle tissue, (4)a decrease in the contractibility of the muscle tissue. Untreated,remodeling typically results in a weakening of the ischemic tissue suchthat it can no longer perform at the same level as the correspondinghealthy tissue. Cardiovascular ischemia is generally a directconsequence of coronary artery disease, and is usually caused by ruptureof an atherosclerotic plaque in a coronary artery, leading to formationof thrombus, which can occlude or obstruct a coronary artery, therebydepriving the downstream heart muscle of oxygen. Prolonged ischemia canlead to cell death or necrosis, and the region of dead tissue iscommonly called an infarct.

In some embodiments, candidate subjects for the methods described hereinwill be patients with stable angina and reversible myocardial ischemia.Stable angina is characterized by constricting chest pain that occursupon exertion or stress, and is relieved by rest or sublingualnitroglycerin. Coronary angiography of patients with stable anginausually reveals 50-70% obstruction of at least one coronary artery.Stable angina is usually diagnosed by the evaluation of clinicalsymptoms and ECG changes. Patients with stable angina may have transientST segment abnormalities, but the sensitivity and specificity of thesechanges associated with stable angina are low.

In some embodiments, candidates for the methods described herein will bepatients with unstable angina and reversible myocardial ischemia.Unstable angina is characterized by constricting chest pain at rest thatis relieved by sublingual nitroglycerin. Anginal chest pain is usuallyrelieved by sublingual nitroglycerin, and the pain usually subsideswithin 30 minutes. There are three classes of unstable angina severity:class I, characterized as new onset, severe, or accelerated angina;class II, subacute angina at rest characterized by increasing severity,duration, or requirement for nitroglycerin; and class III, characterizedas acute angina at rest. Unstable angina represents the clinical statebetween stable angina and acute myocardial infarction (AMI) and isthought to be primarily due to the progression in the severity andextent of atherosclerosis, coronary artery spasm, or hemorrhage intonon-occluding plaques with subsequent thrombotic occlusion. Coronaryangiography of patients with unstable angina usually reveals 90% orgreater obstruction of at least one coronary artery, resulting in aninability of oxygen supply to meet even baseline myocardial oxygendemand. Slow growth of stable atherosclerotic plaques or rupture ofunstable atherosclerotic plaques with subsequent thrombus formation cancause unstable angina. Both of these causes result in critical narrowingof the coronary artery. Unstable angina is usually associated withatherosclerotic plaque rupture, platelet activation, and thrombusformation. Unstable angina is usually diagnosed by clinical symptoms,ECG changes, and changes in cardiac markers.

In some embodiments, candidates for the methods described herein will behuman patients with left ventricular dysfunction and reversiblemyocardial ischemia that are undergoing a coronary artery bypass graft(CABG) procedure, who have at least one graftable coronary vessel and atleast one coronary vessel not amenable to bypass or percutaneouscoronary intervention.

In some embodiments, application of the construct to an ischemic tissueincreases the number of blood vessels present in the ischemic tissue, asmeasured using laser Doppler imaging (see, e.g., Newton et al., 2002, JFoot Ankle Surg, 41(4):233-7). In some embodiments, the number of bloodvessels increases 1%, 2%, 5%; in other embodiments, the number of bloodvessels increases 10%, 15%, 20%, even as much as 25%, 30%, 40%, 50%; insome embodiments, the number of blood vessels increase even more, withintermediate values permissible.

In some embodiments, application of the construct to an ischemic hearttissue increases the ejection fraction. In a healthy heart, the ejectionfraction is about 65 to 95 percent. In a heart comprising ischemictissue, the ejection fraction is, in some embodiments, about 20-40percent. Accordingly, in some embodiments, treatment with the constructresults in a 0.5 to 1 percent absolute improvement in the ejectionfraction as compared to the ejection fraction prior to treatment. Inother embodiments, treatment with the construct results in an absoluteimprovement in the ejection fraction more than 1 percent. In someembodiments, treatment results in an absolute improvement in theejection fraction of 1.5%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%,12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, ormore as compared to the ejection fraction prior to treatment. Forexample, if the ejection fraction prior to treatment was 40%, thenfollowing treatment ejection fractions between 41% to 59% or more areobserved in these embodiments. In still other embodiments, treatmentwith the construct results in an improvement in the ejection fractiongreater than 10% as compared to the ejection fraction prior totreatment.

In some embodiments, application of the construct to an ischemic hearttissue increases one or more of cardiac output (CO) (increases of up to55% or more relative to pre-status treatment), left ventricular enddiastolic volume index (LVEDVI), left ventricular end systolic volumeindex (LVESVI), and systolic wall thickening (SWT). These parameters aremeasured by art-standard clinical procedures, including, for example,nuclear scans, such as radionuclide ventriculography (RNV) or multiplegated acquisition (MUGA), and X-rays.

In some embodiments, application of the construct to an ischemic hearttissue causes a demonstrable improvement in the blood level of one ormore protein markers used clinically as indicia of heart injury, such ascreatine kinase (CK), serum glutamic oxalacetic transaminase (SGOT),lactic dehydrogenase (LDH) (see, e.g., U.S. Publication 2005/0142613),troponin I and troponin T can be used to diagnose heart muscle injury(see, e.g., U.S. Publication 2005/0021234). In yet other embodiments,alterations affecting the N-terminus of albumin can be measured (see,e.g., U.S. Publications 2005/0142613, 2005/0021234, and 2005/0004485;the disclosures of which are incorporated herein by reference in theirentireties).

Additionally, the cultured three-dimensional tissue can be used withtherapeutic devices used to treat heart disease including heart pumps,endovascular stents, endovascular stent grafts, left ventricular assistdevices (LVADs), biventricular cardiac pacemakers, artificial hearts,and enhanced external counterpulsation (EECP).

In a further alternative embodiment that can be combined with any otherembodiments herein, the treating results in production of newcardiomyocytes and new blood vessels in the subject. In a furtheralternative embodiment that can be combined with any other embodimentsherein, the treating results in improvement of left ventricularfunction, fall in end diastolic pressure (EDP) (reduction of up to50-60% or more relative to pre-status treatment), myocardial perfusion,repopulation of the anterior wall with cardiomyocytes, and/or reversingmaladaptive left ventricle remodeling in the subject.

In one non-limiting alternative embodiment in which a synchronouslybeating construct is placed on the heart to aid in contraction of theleft ventricle, beneficial treatment can be demonstrated by animprovement in ejection fraction. In a further non-limiting alternativeembodiment, a non-beating construct is placed on the heart, thenspontaneously begins beating on the heart to aid in contraction of theheart.

The construct can be contacted with the heart in any suitable way topromote attachment. The construct may be attached to various locationson the heart, including the epicardium, myocardium and endocardium, mostpreferably the epicardium. Means for attachment include, but are notlimited to, direct adherence between the construct and the heart tissue,biological glue, suture, synthetic glue, laser dyes, or hydrogel. Anumber of commercially available hemostatic agents and sealants includeSURGICAL® (oxidized cellulose), ACTIFOAM® (collagen), FIBRX®(light-activated fibrin sealant), BOHEAL® (fibrin sealant), FIBROCAPS®(dry powder fibrin sealant), polysaccharide polymers p-GlcNAc (SYVEC®patch; Marine Polymer Technologies), Polymer 27CK (Protein PolymerTech.). Medical devices and apparatus for preparing autologous fibrinsealants from 120 ml of a patient's blood in the operating room in oneand one-half hour are also known (e.g. Vivostat System).

In an alternative embodiment of the invention utilizing directadherence, the construct is placed directly onto the heart and theproduct attaches via natural cellular attachment. In a furtheralternative embodiment, the construct is attached to the heart usingsurgical glue, preferably biological glue such as a fibrin glue. The useof fibrin glue as a surgical adhesive is well known. Fibrin gluecompositions are known (e.g., see U.S. Pat. Nos. 4,414,971; 4,627,879and 5,290,552) and the derived fibrin may be autologous (e.g., see U.S.Pat. No. 5,643,192). The glue compositions may also include additionalcomponents, such as liposomes containing one or more agent or drug(e.g., see U.S. Pat. Nos. 4,359,049 and 5,605,541) and include viainjection (e.g., see U.S. Pat. No. 4,874,368) or by spraying (e.g., seeU.S. Pat. Nos. 5,368,563 and 5,759,171). Kits are also available forapplying fibrin glue compositions (e.g., see U.S. Pat. No. 5,318,524).

In another embodiment, a laser dye is applied to the heart, theconstruct, or both, and activated using a laser of the appropriatewavelength to adhere to the tissues. In alternative embodiments, thelaser dye has an activation frequency in a range that does not altertissue function or integrity. For instance, 800 nm light passes throughtissues and red blood cells. Using indocyan green (ICG) as the laserdye, laser wavelengths that pass through tissue may be used. A solutionof 5 mg/ml of ICG is painted onto the surface of the three-dimensionalstromal tissue (or target site) and the ICG binds to the collagen of thetissue. A 5 ms pulse from a laser emitting light with a peak intensitynear 800 nm is used to activate the laser dye, resulting in thedenaturation of collagen which fuses elastin of the adjacent tissue tothe modified surface.

In another embodiment, the construct is attached to the heart using ahydrogel. A number of natural and synthetic polymeric materials aresufficient for forming suitable hydrogel compositions. For example,polysaccharides, e.g., alginate, may be crosslinked with divalentcations, polyphosphazenes and polyacrylates are crosslinked ionically orby ultraviolet polymerization (U.S. Pat. No. 5,709,854). Alternatively,a synthetic surgical glue such as 2-octyl cyanoacrylate (“DERMABOND”,Ethicon, Inc., Somerville, N.J.) may be used to attach thethree-dimensional stromal tissue.

In an alternative embodiment of the present invention, the construct issecured to the heart using one or more sutures, including, but notlimited to, 5-0, 6-0 and 7-0 proline sutures (Ethicon Cat. Nos. 8713H,8714H and 8701H), poliglecaprone, polydioxanone, polyglactin or othersuitable non-biodegradable or biodegradable suture material. Whensuturing, double armed needles are typically, although not necessarily,used.

In another embodiment, the 3DFC is grown in a bioreactor system (e.g.,U.S. Pat. Nos. 5,763,267 and 5,843,766) in which the framework isslightly larger than the final tissue-engineered product. The finalproduct contains a border, one edge, flap or tab of the scaffoldmaterial, which is used as the site for application of thebiological/synthetic glue, laser dye or hydrogel. In alternativeembodiments, the scaffold weave may be used as an attachment forsuturing or microsuturing.

As used herein, the phrase “an amount effective” means an amount of theconstruct that will be effective to treat the disorder, as discussedherein. As will be clear to those of skill in the art, the methodscomprise the use of one or more of the recited constructs to treatdisorders characterized by a lack of functioning cardiomyocytes. In oneembodiment, the method comprises contacting the heart with an amount ofone or more constructs that serves to cover one or more ischemic regionsof the heart, preferably all ischemic regions of the heart. Theconstruct is used in an amount effective to promote tissue healingand/or revascularization of weakened or damaged heart tissue in anindividual diagnosed with a disorder characterized by a lack offunctioning cardiomyocytes. The amount of the construct administered,depends, in part, on the severity of the disorder, whether the constructis used as an injectable composition (see, US20060154365, incorporatedherein by reference in its entirety), the concentration of the variousgrowth factors and/or Wnt proteins present, the number of viable cellscomprising the construct, and/or ease of access to the heart tissue(s)being treated. Determination of an effective dosage is well within thecapabilities of those skilled in the art. Suitable animal models, suchas the canine model described in US 20060292125 (incorporated byreference herein in its entirety) can be used for testing the efficacyof the dosage on a particular tissue of the heart.

As used herein “dose” refers to the number of cohesive pieces ofconstruct applied to the heart of an individual diagnosed withcongestive heart failure. A typical cohesive piece of construct isapproximately 35 cm². As will be appreciated by those skilled in theart, the absolute dimensions of the cohesive piece can vary, as long itcomprises a sufficient number of cells to promote healing of weakened ordamaged heart tissue in an individual diagnosed with a disordercharacterized by a lack of functioning cardiomyocytes. Thus, cohesivepieces suitable for use in the methods described herein can range insize from 15 cm² to 50 cm².

The application of more than one cohesive piece of construct can be usedto increase the area of the heart treatable by the methods describedherein. For example, in embodiments using a two pieces of cohesiveconstruct, the treatable area is approximately doubled in size. Inembodiments using three cohesive pieces of construct, the treatable areais approximately tripled in size. In embodiments using four cohesivepieces of construct, the treatable area is approximately quadrupled insize. In embodiments using five cohesive pieces of construct, thetreatable area is approximately five-fold, i.e. from 35 cm² to 175 cm².

In some embodiments, one cohesive piece of construct is attached to aregion of the heart in an individual diagnosed with a disordercharacterized by a lack of functioning cardiomyocytes.

In other embodiments, two cohesive pieces of construct are attached to aregion of the heart in an individual diagnosed with a disordercharacterized by a lack of functioning cardiomyocytes.

In other embodiments, three cohesive pieces of construct are attached toa region of the heart in an individual diagnosed with a disordercharacterized by a lack of functioning cardiomyocytes.

In other embodiments, four, five, or more cohesive pieces of constructare attached to a region of the heart in an individual diagnosed with adisorder characterized by a lack of functioning cardiomyocytes.

In embodiments in which two or more cohesive pieces of construct areadministered, the proximity of one piece to another can be adjusted,depending in part on, the severity of the disorder characterized by alack of functioning cardiomyocytes, the extent of the area beingtreated, and/or ease of access to the heart tissue(s) being treated. Forexample, in some embodiments, the pieces of 3DFC can be locatedimmediately adjacent to each other, such that one or more edges of onepiece contact one or more edges of a second piece. In other embodiments,the pieces can be attached to the heart tissue such that the edges ofone piece do not touch the edges of another piece. In these embodiments,the pieces can be separated from each other by an appropriate distancebased on the anatomical and/or disease conditions presented by thesubject. Determination of the proximity of one piece to another, is wellwithin the capabilities of those skilled in the art, and if desired canbe tested using suitable animal models, such as the canine modeldescribed in US20060292125.

In embodiments that comprise a plurality of pieces of construct, some,or all of the pieces can be attached to the same or different areas ofthe heart.

In embodiments that comprise a plurality of pieces of construct, thepieces are simultaneously attached, or concurrently attached to theheart.

In some embodiments, the construct pieces are administered over time.The frequency and interval of administration depends, in part, on theseverity of the disorder, whether the 3DFC is used as an injectablecomposition (see, US20060154365, incorporated herein by reference in itsentirety), the concentration of the various growth factors and/or Wntproteins present, the number of viable cells comprising the 3DFC, and/orease of access to the heart tissue(s) being treated. Determination ofthe frequency of administration and the duration between successiveapplications is well within the capabilities of those skilled in theart, and if desired, can be tested using suitable animal models, such asthe canine model described in US20060292125.

In a further alternative embodiment, one or more construct is contactedwith the left ventricle. In a further alternative embodiment, the one ormore constructs cover the entire heart.

In embodiments that comprise a plurality of pieces of construct, some,or all of the pieces can be attached to the area comprising the heart.In other embodiments, one or more of the construct pieces can beattached to areas that do not comprise damaged myocardium. For example,in some embodiments, one piece can be attached to an area comprisingischemic tissue and a second piece can be attached to an adjacent areathat does not comprise ischemic tissue. In these embodiments, theadjacent area can comprise damaged or defective tissue. “Damaged,” or“defective” tissue as used herein refer to abnormal conditions in atissue that can be caused by internal and/or external events, including,but not limited to, the event that initiated the ischemic tissue. Otherevents that can result in ischemic, damaged or defective tissue includedisease, surgery, environmental exposure, injury, aging, and/orcombinations thereof.

In embodiments that comprise a plurality of pieces of culturedthree-dimensional tissue, the construct pieces can be simultaneouslyattached, or concurrently attached to an ischemic tissue.

In an alternative embodiment that can be combined with any otherembodiment disclosed herein, the cardiomyocytes or precursors thereofare adhered to the 3DFC at a cell density ranging between 0.5×10⁶cells/cm² and 5×10⁶ cells/cm²; more preferably between 1×10⁶ cells/cm²and 4×10⁶ cells/cm²; and most preferably between 1.5×10⁶ cells/cm² and3×10⁶ cells/cm². In another embodiment that can be combined with anyother embodiment disclosed herein, the cardiomyocytes or precursorsthereof are seeded on the construct at a density between 1.5×10⁶cells/cm² and 3×10⁶ cells/cm², and the fibroblasts are present on theconstruct at a density of between about 8.0×10⁵ cells/cm² and about2.0×10⁶ cells/cm².

In various embodiments, the cardiomyocytes or precursors thereof arepresent in a ratio with fibroblasts on the construct of between about1:10 and about 10:1; about 1:9 to about 9:1; about 1:8 to about 8:1;about 1:7 to about 7:1; about 1:6 to about 6:1; about 1:5 to about 5:1;about 1:4 to about 4:1; about 1:3 to about 3:1; about 1:2 to about 2:1;or about 1:1. Other ratios of cells are also possible.

In a further alternative embodiment that can be combined with any otherembodiment herein, the cardiomyocytes or precursors thereof areengineered to express a therapeutic of interest, such as thymosin beta-4(TB4), akt murine thyoma viral oncogene homolog (AKT1), stromacell-derived factor-1 alpha (SDF-1), and hepatocyte growth factor (HGF).Alternatively, one or more of thymosin beta-4 (TB4), akt murine thyomaviral oncogene homolog (AKT1), stroma cell-derived factor-1 alpha(SDF-1), and hepatocyte growth factor (HGF) can be added exogenously tothe construct prior to implantation. (RegeneRx Biopharmaceuticals, Inc.(Bethesda, Md.) In this embodiment, the cardiomyocytes or precursorsthereof will provide new cardiomyocytes to grow onto the damaged heartand the added factor(s) will augment cell migration and engraftment.

In various alternative embodiments, the cardiomyocytes or progenitorsthereof are selected from the group consisting of cardiomyocytes,cardiac stem cells (such as c-kit+ cardiac stem cells, CD34+ endothelialprogenitor cells, autologous bone marrow cells, and mesenchymal stemcells. In an alternative embodiment that can be combined with any otherembodiment disclosed herein, the cardiomyocytes or precursors thereofare human cells, more preferably human cells derived from (ie, obtainedfrom and possibly expanded ex vivo prior to administration) the subjectto be treated (such as by standard biopsy or other surgical procedures).

The methods may further comprise systemic administration of cytokines tothe subject, including but not limited to Insulin like growth factor(IGF), Hepatic Growth Factor (HGF), and Stromal cell-derived factor a(SDF-1a).

The methods and compositions described herein can be used in combinationwith conventional treatments, such as the administration of variouspharmaceutical agents and surgical procedures. For example, in someembodiments, the cultured three-dimensional tissue is administered withone or more of the medications used to treat a disorder characterized bya lack of functioning cardiomyocytes. Medications suitable for use inthe methods described herein include angiotensin-converting enzyme (ACE)inhibitors (e.g., enalapril, lisinopril, and captopril), angiotensin II(A-II) receptor blockers (e.g., losartan and valsartan), diuretics(e.g., bumetanide, furosemide, and spironolactone), digoxin, betablockers, and nesiritide.

Additionally, the constructs can be used with other options used totreat a disorder characterized by a lack of functioning cardiomyocytes,including heart pumps, also referred to as left ventricular assistdevices (LVADs), biventricular cardiac pacemakers, cardiac wrap surgery,artificial hearts, and enhanced external counterpulsation (EECP), andcardiac wrap surgery (see, e.g., U.S. Pat. Nos. 6,425,856, 6,085,754,6,572,533, and 6,730,016, the contents of which are incorporated hereinby reference).

In some embodiments, the construct is used in conjunction with cardiacwrap surgery. In these embodiments, a flexible pouch or jacket is usedto deliver and/or attach the construct, which can be placed inside orembedded within the pouch prior to placement over the damaged orweakened heart tissue. In other embodiments, the pouch and the 3DFC canbe joined together. For example, the pouch and the construct can bejoined together using a stretchable stitch assembly. In otherembodiments, the construct can be configured to comprise threads usefulfor joining the framework to the pouch. U.S. Pat. Nos. 6,416,459,5,702,343, 6,077,218, 6,126,590, 6,155,972, 6,241,654, 6,425,856,6,230,714, 6,241,654, 6,155,972, 6,293,906, 6,425,856, 6,085,754,6,572,533, and 6,730,016 and U.S. Patent Publication Nos. 2003/0229265,and 2003/0229261, the contents of which are incorporated herein byreference, describe various embodiments of pouches and jackets, e.g.,cardiac constraint devices, that can be used to deliver and/or attachthe construct.

In some embodiments, other devices, in addition to the construct areattached to the pouch, e.g., electrodes for defibrillation, a tensionindicator for indicating when the jacket is adjusted on the heart to adesired degree of tensioning, and used in the methods and compositionsdescribed herein. See, e.g., U.S. Pat. Nos. 6,169,922 and 6,174,279, thecontents of which are incorporated herein by reference.

A number of methods can be used to measure changes in the functioning ofthe heart in subjects before and after attachment of the construct. Forexample, an echocardiogram can be used to determine the capacity atwhich the heart is pumping. The percentage of blood pumped out of theleft ventricle with each heartbeat is referred to as the ejectionfraction. In a healthy heart, the ejection fraction is about 60 percent.In an individual with chronic heart failure caused by the inability ofthe left ventricle to contract vigorously, i.e., systolic heart failure,the ejection fraction is usually less than 40 percent. Depending on theseverity and cause of the heart failure, ejection fractions typicallyrange from less than 40 percent to 15 percent or less. An echocardiogramcan also be used to distinguish between systolic heart failure anddiastolic heart failure, in which the pumping function is normal but theheart is stiff.

In some embodiments, echocardiograms are used to compare the ejectionfractions before and following treatment with the construct. In certainembodiments, treatment with the construct results in improvements in theejection fraction between 3 to 5 percent. In other embodiments,treatment with the construct results in improvements in the ejectionfraction between 5 to 10 percent. In still other embodiments, treatmentwith the construct results in improvements in the ejection fractiongreater than 10 percent.

Nuclear scans, such as radionuclide ventriculography (RNV) or multiplegated acquisition (MUGA) scanning can be used to determine how muchblood the heart pumps with each beat. These tests are done using a smallamount of dye injected in the veins of an individual A special camera isused to detect the radioactive material as it flows through the heart.Other tests include X-rays and blood tests. Chest X-rays can be used todetermine the size of the heart and if fluid has accumulated in thelungs. Blood tests can be used to check for a specific indicator ofcongestive heart failure, brain natriuretic peptide (BNP). BNP issecreted by the heart in high levels when it is overworked. Thus,changes in the level of BNP in the blood can be used to monitor theefficacy of the treatment regime.

In a further aspect, the present invention provides kits for treatingCHF, comprising a suitable construct as disclosed above and a means forattaching the construct to the heart or organ. The means for attachmentmay include any such attachment device as described above, for example,a composition of surgical glue, hydrogel, or preloaded prolene needlesfor microsuturing.

EXAMPLES Example 1. 3DFC Seeding and Co-Culture

The 3DFC patch is a cryopreserved human fibroblast-derived tissuecomposed of fibroblasts, extracellular matrix, and a bioabsorbablescaffold (21,22). The fibroblast cells were from a qualified cell bank;tested for animal viruses, retroviruses, cell morphology, karology,isoenzymes, and tumorgenicity, free from viruses, retroviruses,endotoxins and mycoplasma. The 3DFC was supplied frozen (5 cm×7.5 cm);it at −75°±1 0° C. until ready for use when it was placed in sterile PBS(34-37° C.) and applied to the heart within 60 minutes of removal.

Random seeding: The 3DFC (ANGINERA™ obtained from and thawed perTheregen, Inc. protocols) was cut into near circular sectionsapproximately 1.5 cm in diameter to fill the well space of a 24 wellculture plate. After the 3DFC was placed in the bottom of the well andcompletely covering its base, 1.5 ml of media (10% FBS in DMEM-LG)containing >3×10⁶ enothelial progenitor cells (rat neonatalcardiomyocytes) were added in suspension over the 3DFC at 27° C. Theplate containing the 3DFC and cellular suspension was then centrifugedat 1300 rpms for 5 min forcing the cells in suspension into the 3DFC at27° C. The plate containing the 3DFC was then transferred to a cellincubator and incubated 24 hrs at 37° C. and 5% CO₂ to allow furthercellular adhesion and proliferation (FIG. 1).

Adhesion of the desired cells onto the 3DFC was greatly enhanced when>3×10⁸ cells/ml are added in suspension. At this concentration there wasa “traffic jam effect” that takes place causing all the cells insuspension to come in contact with the 3DFC at the same time thusclogging any openings in the 3DFC not allowing the added cells to passthru.

Starting out with a large number of cells allowed all cells insuspension to migrate unto the 3DFC, the more cells that make contactwith the 3DFC enabled some cells to pass through the pores ending upwith 1.5 to 2 million cells seeded on the patch.

Cell Sheet Seeding: Endothelial progenitor cells (bovine pulmonaryarterial endothelial cells (BPAECS)) were grown in 24 well or 6 wellculture plate (CellSeed, Japan) until they were confluent. The cultureplates were then chilled to 20° C. allowing disassociation of the cellsheet from the culture plate. After 40 min the sheet was fullydisassociated (FIGS. 2 & 3), and using a 5 ml, 10 ml, or 1000 ul pipettethe disassociated cell sheet was taken up in existing culture media andtransferred directly onto the 3DFC (obtained from and thawed perTheregen Inc. protocols).

Using 2-3 ul droplets of culture media dripped onto the new cell sheet(at 27° C.), the cell sheet unfolded to lay flat against the 3DFC. Onceflat and flush against the 3DFC, the cell sheet+3DFC complex wasincubated at 37° C. and 5% CO₂ for 10 min without additional mediaallowing for full adhesion of the cell sheet to the 3DFC. After, theseeded 3DFC was incubated over night prior to use (implantation, etc.).

Harvested cells sheets retained all cellular adhesion molecules andself-adhered when placed on the 3DFC. In addition, this method of cellharvesting kept intact all cell-to-cell interactions.

Example 2. Construction of a Spontaneously Contracting BiologicallyActive Cardiomyocyte Scaffold

Methods: Cardiomyocytes were isolated from neonatal rats 1-2 days oldand seeded onto 3DFC scaffolds that were cut into pieces ofapproximately 1.5-1.7 cm² in diameter. (ANGINERA™, obtained fromTheregen, Inc) at concentrations ranging from 0.6×10⁶ to 2.7×10⁶cells/cm². Briefly, the hearts were excised, atria removed andventricles cut into 0.5-1 mm portions, minced, then digested in apancreatin/collagenase solution. Following each enzymatic digest,cardiomyocytes were collected, combined and re-suspended in DMEM with10% FBS. Lastly, the suspension was differentially plated in Ham's F-12with 100 mg/ml BSA. The neonatal cardiomyocyte-3DFC were culturedbetween 1-10 days at 37° C. with 5% CO₂ in 10% FBS in DMEM-LG. Media waschanged 24 hrs after initial plating then every 48 hrs.Results: Higher density cardiomyocyte seedings (1.8×10⁶ to 2.7×10⁶cells/cm²) of the 3DFC showed synchronized and spontaneous contractionsof the entire scaffold after 48 hrs in culture. Contractions increasedin robustness from 48 hrs to 5 days. Lower density cardiomyocyteseedings (0.6-1.2×10⁶ cells/cm²) displayed non-synchronized yetspontaneous contractions. At 72 hours these contractions begansynchronizing and by 84 hours, cell contractions were fully synchronizedbut contracted in a non-consistent manner. At 5 days, scaffolds seededwith 2.7×10⁶ cells/cm² contracted in a consistent rhythmic anddirectional fashion (ie: medially, with each patch beating in arepetitive directional motion, squeezing “inwards”). Contractions wererecorded at 71±3 beats BPM with a mean displacement of 2.9±0.1 mm andcontraction velocity of 3.4±0.5 mm/sec (N=10).Conclusion: These findings showed that isolated cardiomyocytes can beseeded and co-cultured onto a biodegradable 3-dimensional construct in amanner allowing cellular survival, communication and electricalcoupling. These claims are supported by the observation that the newlyseeded neonatal cardiomyocyte-3DFC scaffolds beat spontaneously and in asynchronized, directional fashion with no electrical stimulation. Thisnewly formed neonatal cardiomyocyte 3DFC scaffold is a new and uniquecell delivery system to treat CHF.

Example 3 Cellular Communications/Alignment

This example describes cardiomyocyte alignment on cardiomyocyte seeded3DFC patches and in vivo improvements in rats with heart failure withtreatment using the described cardiomyocyte seeded 3DFC (NCM-3DFC).

Connexin Formation: As shown above, isolated cardiomyocytes can beseeded and co-cultured onto the 3DFC; that these seeded patches contractspontaneously and rhythmically. In theory, rhythmic contractions supportthe hypothesis that the seeded cardiomyocytes align and establishcomplex connections with each other allowing for electromechanicalcellular communication. These connections, known as connexins, areessential for the rhythmic contraction of cardiac muscle.Cellular Injections: The following example shows connexin formation 24hrs after cardiomycocyte seeding (same cell type as in example 2) andincreased cellular connectiveness through connexin formation over time,up to 6 days, thus demonstrating connexin functionality within the 3DFC.In short, dye transfer was evaluated in both 3DFC and NCM-3DFC culturedfor 6 days. Three dyes were injected simultaneously: [2-(4-nitro-2, 1,3-benzoxadiol-7-yl)aminoethyl]trimethylammonium (NDB-TMA; mol wt 280,net charge 1+, 10 mM), Alexa 350 (mol wt 326, net charge 1-, 10 mM), andRhodamine Dextran (0.1 mg/ml). Microelectrode tips were created from 1.0mm filament glass (A-M Systems, Everett, Wash.) on a Sutter Instrumentspuller (Novato, Calif.). Tips were filled by capillary action with amixture of the three dyes, backfilled with 200 mM KCl, and then loweredonto cell surface. Dye was slowly and continuously injected bycapacitance overcompensation of the amplifier (A-M Systems). Photos weretaken every 30 seconds (up to 2.5 min) then every 2.5 minutes up to 20minutes. Cells that received dye from the injected cell after 10 minuteswere compared between groups. Injections into cardiomyocyte seededpatches resulted in extensive dye passage between seeded cardiomyocytes(FIG. 4), demonstrating the functional presence of connexins. Non-seededpatches (fibroblasts only) resulted in retention of dye strictly in theprimary cell, with no passage of dye into neighboring cells.Furthermore, addition of halothane, inhibited connexin activity asrepresented by disruption of dye transfer between cells (FIG. 4).Histological Assessment: Additionally, histological assessment ofcardiomyocyte seeded patches between 1, 4 and 8 days after seedingdemonstrate that seeded cardiomyocytes adhere to the 3DFC and proceed toalign on the surface of the 3DFC. The cardiomyocytes remain on the outersurface of the 3DFC, on the seeded face over time (one to eight days)and do not migrate into the 3DFC or to the opposite, non-seed side.(FIGS. 8-11) Cells centrifuged onto the patch were found to residebetween the fibers of the 3DFC.Echocardiography and Hemodynamics: Rats were infarcted using standardtechniques in our laboratory. In short, a permanent ligature was placedaround the left coronary artery of rats and the animals allowed torecover for three weeks. During this recovery time, rats developedchronic heart failure (CHF); classically defined as depressed ejectionfraction and cardiac output, elevated end-diastolic pressure and volumewith increased left ventricular chamber dimensions. Chronic heartfailure rats were divided at random into control (no treatment) andtreatment (cardiomyocyte seeded 3DFC) groups 3 weeks after coronaryligation. Both control and treatment groups were studied at baseline,seeded 3DFC was applied 3 weeks post MI, and studied all rats werestudied 6 weeks post MI (3 weeks post implant of seeded 3DFC). Ratsreceived 3 and 6 week echocardiography in addition to 6 weekhemodynamics. (FIGS. 5-7)

Graphical data of these (EF, CI, EDP) show changes/improvements withstatistical (p<0.05) analysis between groups as denoted. Data wereexpressed as mean±standard error (SE). For the physiologic andechocardiographic measurements, the Student t test was used for singlecomparison of sham versus other study groups. Interactions were testedusing two-way analysis of variance (ANOVA), intergroup differences wereevaluated using the Student-Newman-Keuls test for statisticalsignificance (P≤0.05).

Using methods previously described, cardiomyocytes were isolated andseeded onto the 3DFC and incubated overnight. Cardiomyocyte seeded 3DFCwere then sutured directly onto the epicardial portion of the rat'sinfarcted left ventricle. The rat's chest was closed and the animalallowed to recover. Echocardiography data demonstrates improvements inejection fraction (25%) and cardiac output (55%) in treated vs.non-treated rats (FIGS. 5 & 6), thus demonstrating the use of theconstructs of the invention for treating CHF.

We claim:
 1. A method for treating a disorder characterized by a lack offunctioning cardiomyocytes, comprising contacting the heart of a subjectsuffering from such a disorder with an amount effective to treat thedisorder of a construct comprising cardiomyocytes, cardiac stem cells,or progenitors thereof adhered to a three dimensional fibroblastconstruct (3DFC), wherein the construct is capable of spontaneoussynchronized contractions across the 3DFC; and wherein thecardiomyocytes, cardiac stem cells, or progenitors thereof are seeded onthe construct at a density of between 0.5×10⁶ cells/cm² and 5×10⁶cells/cm² and/or the cardiomyocytes, cardiac stem cells, or progenitorsthereof are present in a ratio of between about 1:10 and about 10:1 withfibroblasts on the 3DFC.